Serious skin disorders count among the most devastating health conditions and most difficult treatment challenges. These arise both from genetic diseases and from injuries, such as the often-debilitating long-term suffering of the >500,000 serious burn victims who are hospitalized every year in the US alone. Today's top treatments, including major skin grafts, still struggle to overcome the key natural limitations of human skin's relatively basic repair processes. While these generally restore structural integrity, they often result in extensive scarring that not only causes disfigurement and accompanying psychological trauma, but also significant loss of functionality, including impaired sensitivity and increased susceptibility to infection. The development of more effective skin therapies now stands to benefit greatly from emerging new understanding of the remarkable healing abilities exhibited by naturally regenerative vertebrates. To this end, our longstanding work on the ?axolotl? salamander, the champion among such species, is identifying critical molecules, regulatory pathways and cellular processes underlying scar-free regeneration. Here, we will these address central issues in skin regeneration using cutting edge screening and analysis tools in axolotl.
The aim of the project is to: 1) define the exact role of Sall4 in the dermis and epidermis for promoting scar free skin regeneration. 2) harness skin cell transcriptome data to define and functionally elucidate the role of different skin cell populations in regulating scar free regeneration. 3) We will translate our findings of the role of SALL4 in regulating collagen in axolotls into an in vitro model of human skin regeneration and use this new knowledge to attempt to promote scar- free wounding healing in human cells. In summary, these experiments will reveal and characterize key differences between the axolotl's regenerative and the mammal's non-regenerative responses to injury, identifying molecules and pathways required for the former to assess their potential for enhancing the latter. The ultimate aim of these studies is thus to improve quality of life for people with chronic open wounds and dysfunctional scar tissue.

Public Health Relevance

Public Health Relevance Open wounds or scar tissue caused due to genetic skin diseases or as a result of traumatic burn or blast injuries have a devastating effect on people's lives and pose a huge financial burden. In summary, these experiments will unravel key pathways necessary to promote scar-free wounding healing in axolotl skin and will inform us of the key signaling pathways that must be regulated to attempt a similar response in mammalian skin. The ultimate aim of these studies is thus to improve quality of life for people with open wounds and debilitating scar tissue.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD092451-01
Application #
9364818
Study Section
Development - 1 Study Section (DEV1)
Program Officer
Mukhopadhyay, Mahua
Project Start
2017-08-01
Project End
2022-05-31
Budget Start
2017-08-01
Budget End
2018-05-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Genetics
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Echeverri, Karen; Zayas, Ricardo M (2018) Regeneration: From cells to tissues to organisms. Dev Biol 433:109-110
Erickson, Jami R; Echeverri, Karen (2018) Learning from regeneration research organisms: The circuitous road to scar free wound healing. Dev Biol 433:144-154